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Decontamination of Industrial Waste Water by

Photocatalytic Oxidation of Organic Components:

A Model Study

Industrial waste water which was highly loaded by chlori- nated (50 mg A O X l "1) and other organic compounds was decontaminated by laboratory-scale photooxidation of these organic impurities in the presence of oxygen and ti- tanium dioxide as photocatalyst. The disappearance of the organic compounds was determined as a function of the irradiation time. Some contaminants such as chlorobenzene, trichloroethylene and trichloromethane were photolyzed separately in order to obtain information on the course and stoichiometry of the photooxidation.

By Frank Sabin, Thomas Türk, and Arnd Vogler*

Reinigung von Industrieabwasser durch photokataly- tische Oxidation der organischen Verbindungen (Modell- studie). Industrieabwasser, das mit chlorierten (50 mg A O X 1 ') und anderen organischen Verbindungen hoch belastet war, wurde durch Photooxidation im Labormaßstab in Ge- genwart von Sauerstoff und Titandioxid als Photokataly- sator gereinigt. Die Abnahme der organischen Verbindun- gen wurde als Funktion der Belichtungszeit bestimmt. E i - nige Schadstoffe wie Chlorbenzol, Trichlorethylen und Trichlormethan wurden einzeln photolysiert, um Informa- tionen über den Ablauf und die Stöchiometrie der Photo- oxidationen zu erhalten.

1 Introduction

The removal of chlorinated organic compounds from waste water is a difficult problem because these substances are not accessible to conventional decontamination procedures. The photooxidation by oxygen with semiconductor materials such as T i 02 as photocatalyst seems to be a promising method to effectively remove organic impurities from waste water. Previous studies have shown that a variety of organic compounds including chlorinated materials can be pho- tooxidized in water on a laboratory scale [1 —8]. In some cases it was demonstrated that the photomineralization to H20 , C 02 and H C l was complete [1, 3, 9 - 1 2 ] . Presently, attempts are being made to extent this process from a lab- oratory to a technical scale [13 — 15].

Generally the photocatalytic oxidation has been studied for model solutions which contain only a single organic com- pound while industrial waste water which may contain a wide variety of organic pollutants has not been subjected to this photocatalysis. In the present investigation we studied the applicability of this method to the purification of in- dustrial waste water. The efficiency was evaluated by a k i - netic analysis. The consumption of the organic compounds was determined as a function of the irradiation time. Since a complete analysis of all organic compounds was not avail- able their concentration was determined by the group pa- rameter T O C (total organic carbon).

Larger organic molecules are certainly not photooxidized in one step. Accordingly, intermediates which could be even more toxic than the original contaminant may be generated during the photooxidation. Unfortunately, in the majority of previous studies the photooxidation was monitored only by the disappearance of the substrate. However, an addi- tional time dependent analysis of the products would pro- vide valuable information on the course and stoichiometry of the photolysis. According to these considerations we stud- ied the photooxidation of the contaminants chlorobenzene,

* D r . F . S a b i n , D r . T h . T ü r k , Prof. D r . A . Vogler, Institut für A n - organische C h e m i e der U n i v e r s i t ä t Regensburg, U n i v e r s i t ä t s - s t r a ß e 31, 8400 Regensburg

benzene, trichloroethylene and trichloromethane in separate experiments. The consumption of the reactants as well as the formation of C O: was determined as function of the irradiation time.

2 Experimental Section

Materials and Reagents: The photocatalyst T i O: P-25 was used as supplied by Degussa. This material was mainly an- atase. The BET-surface was 55 + 15 m: g" 1 according to the supplier. The average particle size was 30 nm. Doubly distilled water was chosen as general solvent.

The industrial waste water was supplied by Wacker-Chemie G m b H , Burghausen. Samples were collected from the feed of the sewage treatment plant (waste water A) and from waste water which came from the production of silicones (waste water B). Waste water A contained pollutants from the production of polymers (Polyvinylchloride and polyvi- nylacetate), chlorinated solvents and silicones. Chlorinated organic components were essential constituents of all waste water samples [16]. The concentration of some selected compounds and group parameters are given in Table 1. All samples were deep-frozen immediately after being collected to avoid loss of contaminants by evaporation and chemical reaction prior to photolysis.

Chlorobenzene (p.a.), trichloroethylene (p.a.) and benzene (p.a.) were supplied by Merck, trichloromethane (99%) was supplied by Aldrich. All substrates were used without further purification.

Photolysis: As photolysis cell Perkin-Elmer HS-6 round ves- sels (length 3.7 cm, diameter 2 cm) were used which could be sealed gas tight with a septum. The cell transmitted light above 320 nm. The photolysis cell contained 2 ml of sample solution, 2.0 mg T i O: and a small stirrer. For the photolysis of chlorobenzene, benzene, trichloroethylene and trichlo- romethane in separate experiments the concentrations of the aqueous solutions were 1.0 m M . Irradiation of all samples was carried out in a Photon Technology International setup equipped with a 450 W Xenon lamp (Osram). The light beam was focused on the photolysis cell by an elliptic mirror.

Z. Wasser- Abwasser-Forsch. 25, 163-167 (1992) < V C H Verlagsgesellschaft m b H , D-6940 Weinheim, 1992 0044-3727 92 0307-0163 S 03.50+.25 0 163

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The p H of the industrial waste water samples was adjusted to 8 by adding N a O H before irradiation. Due to the limited supply of oxygen in the sealed photolysis cells the concen- trations of organic material were generally adjusted to the amount of available oxygen [17] in order to achieve com- plete photooxidation. Solutions of chlorobenzene, benzene, trichloroethylene and trichloromethane were left at their natural p H . All samples were vigorously stirred during pho- tooxidation (Ika Combimag R C T magnetic stirrer, 1100 r.p.m.) to keep the catalyst suspended and to achieve a suf- ficient transfer of oxygen from the gas to the liquid phase.

A l l photolyses were carried out three times. Blank solutions were kept in the dark for comparison. Photooxidation rates were reproducible to within ± 5 % .

Analyses: Carbon dioxide produced during the photolyses was measured by head-space gas chromatography (Perkin- Elmer gas Chromatograph 8500 equipped with a HS-6 head- space analyzer, hot-wire detector, a packed column (2 m, 1/8 in. diameter, Porapak Q, 100—120 mesh) and helium as carrier gas). The gas chromatographic measurements were calibrated by the reaction of N a2C 03 with H C l .

The T O C of the waste water samples was determined as C 02 by G C after oxidation of all organic components by K2S208 (90 C, 120 min). The loss of T O C during the pho- tolysis was calculated from the amount of C 02 generated photochemically.

Aqueous solutions of chlorobenzene, benzene, trichloroeth- ylene and trichloromethane which were photolyzed in sep- arate experiments were also analyzed by G C as described elsewhere [18]. The oxygen consumption during photoox- idation was measured gas chromatograpically (Perkin Elmer gas Chromatograph as described above with packed column 2 m, 1/8 in. diameter, molecular sieve 5Ä, 60 — 80 mesh).

For calibration the initial concentration of oxygen in the aqueous solution was taken from literature data [17].

3 Results and Discussion

General: The photocatalytic oxidation of a wide variety of organic compounds in aqueous solution has been reported.

The irradiation of the suspended powder of the semicon- ductor such as T i 02 (k < 390 nm [19]) leads to the sepa- ration of electrons and holes. Both are capable to react with species adsorbed onto the surface of the semiconductor par- ticles. While electrons may reduce adsorbed oxygen to O f the hole can oxidize adsorbed water or hydroxide ions to O H ' radicals. These hydroxyl radicals are powerful oxidants which are able to oxidize many substrates at the semicon- ductor surface [3, 7, 8, 20 — 23]. It has been shown that organic compounds such as chlorocarbons are completely photomineralized according to the overall stoichiometry (1) [1, 3, 1 0 - 1 2 , 2 4 - 2 6 ] :

hv

CnHmC ly + x 02 >nC02 + y H C l + w H20 (1) The time dependent turnover can be determined by meas-

uring the decrease of the substrates [18, 27, 28] and/or the increase of products [3, 5, 18, 24]. From these data the efficiency and the course of the photolysis can be evaluated on the basis of a suitable kinetic analysis. For the hetero- geneous photocatalysis with semiconductor particles several approaches have been applied. The Langmuir-Hinshelwood kinetics [1, 3, 8, 10, 21, 25, 2 8 - 3 1 ] provides a general model which is applicable to a large concentration range. Accord- ing to this model all reactive catalytic sites of the semincon- ductor surface are occupied when the concentration of sub-

strate is high. Therefore the efficiency of the photooxidation is limited by the number of catalytic sites available. This results in a zeroth-order kinetics. At lower concentration of substrate however, the degradation is proportional to the concentration. The reaction is now limited by diffusion to the semiconductor surface. This may result in a pseudo first- order kinetics.

These predictions were indeed confirmed experimentally.

The decrease of substrate has been found to follow pseudo- first order kinetics if substrate concentration was low [11, 12, 18, 21, 23, 26, 2 8 - 3 0 , 32, 33]. On the contrary, at high concentrations a zeroth-order kinetics was observed [18, 31, 33].

However, any simple kinetic model can not take into ac- count special effects such as the competition of different substrates for the catalytic sites [10, 31]. In addition, an insufficient and declining oxygen supply causes complica- tions which can be encountered in closed systems as used in our experiments.

0 20 40 60 80 irradiation time (min)

F i g u r e 1: P h o t o o x i d a t i o n of waste water A w i t h 563 m g T O C l "1 ( A) , waste water A (1:10) with 52 m g T O C 1 ~1 ( • ) a n d waste water B (1:10) w i t h 100 m g T O C T1 ( • )

0 20 40 60 80 100 120 irradiation time (min)

F i g u r e 2: P h o t o o x i d a t i o n of waste water A (1:10) w i t h 52 m g T O C 1 1

Industrial Waste Water: At high substrate concentrations a plot turnover versus irradiation time should result in a straight line in accord with a zeroth-order kinetics. At later stages of the photolysis a curve should be observed since the substrate concentration has reached the range of pseudo- first order kinetics. Finally, the concentration approaches a limiting value which may correspond to 100% turnover.

Such a characteristic behavior was not observed for waste

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water A (Fig. 1) since the amount of oxygen in the sealed photolysis cell was insufficient for a complete photooxida- tion [17]. However, when waste water A was diluted 1:10 the oxygen supply was sufficient and the plot showed the expected behavior (Fig. 1, 2). Similar results were obtained with diluted waste water B (Fig. 1, 3).

0 20 40 60 80 100 120 irradiation time (min)

F i g u r e 3: P h o t o o x i d a t i o n of waste water B (1:10) with 100 mg T O C 1 r

T a b l e 1: A n a l y t i c a l characterization of waste water samples [16]

C o n t a m i n a n t [ m g 1 ']

Waste Water A Waste Water B

C h l o r o b e n z e n e <0.1 0.5

1,1 - D i c h l o r o e t h y l e n e <0.1 <0.1

trans 1,2-Dichlorocthylcnc <().! <().!

eis 1.2-Dichloroethylene <0.1 <0.1

Trichloroethylene <0.1 <().l

Tetrachloroethylenc <0.1 <().!

C h l o r o m e t h a n e 2.4 13

C h l o r o e t h a n c 2.5 11

D i c h l o r o m e t h a n e 4.6 2.6

T r i c h l o r o m e t h a n e 0.3 <0.1

Tetrachloromcthane <0.1 <0.1

A O X 44.3 55.0

P O X 6.2 22 2

T O C 563 1020

C O D 1352 2539

p H 4.6 1.2

A O X : adsorbablc organic halides; P O X : purgcablc organic halidcs:

T O C : total organic c a r b o n : C O D : chemical oxygen d e m a n d

The inspection of Fig. 2 and 3 reveals more details. The organic constituents of diluted waste water A were almost completely photooxidized after an irradiation of 60 min (Fig.

2). After 120 min a limiting value of 92% photooxidation was reached. The residual T O C may be due to compounds such as perchlorinated alkanes (Table 1) which are pho- tooxidized very slowly or not at all [1, 18]. Diluted waste water B showed an additional deviation (Fig. 3). Two ranges of zeroth-order behavior can be identified. The first of this region extends from 0 to about 20 min and the second from about 70 to 120 min. In the beginning an efficient photolysis took place which was almost complete after 45 min irradi- ation time. At later stages a less efficient photolysis occurred.

Both ranges can be assigned most likely to two different compounds or groups of compounds which are photooxi-

dized with sufficiently different efficiencies. Even after an irradiation of 180 min the photooxidation of the organic constituents of diluted waste water B was not yet complete (83%).

Selected Chlorinated Organic Compounds: In the previous section it has been demonstrated that mixtures of chlori- nated organic compounds can be photooxidized efficiently although it is difficult to gain a deeper insight in the course of the photolysis under these conditions. More details are revealed if single compounds instead of mixtures are pho- tooxidized. We explored this possibility and selected typical chlorinated organic compounds for this purpose. In addition to the disappearance of the substrate the formation of C O: as photooxidation product was determined in order to de- tect the generation of intermediates and to analyze the stoi- chiometry of the photolyses.

For the photolysis of chlorobenzene the decrease of this substrate did not match the C O: production during the first 100 min of irradiation (Fig. 4). An explanation for this ob- servation is provided in Fig. 5. In addition to the decrease of the substrate the difference between this decrease and the increase of stoichiometric amounts of C O: was plotted ver- sus irradiation time. This difference gives evidence for the formation of intermediates which are generated from the beginning, reach a maximum concentration after 10 min, undergo themselves a photooxidation and are completely photooxidized at the end (120 min). It is quite understand- able that larger molecules such as chlorobenzene are not photooxidized in one step.

0 20 40 60 80 100 irradiation time (min)

Figure 4: P h o t o o x i d a t i o n of chlorobenzene calculated by decrease in substrate ( • ) and increase in C O: ( • )

0 10 20 30 40 50 60 70 80 90 irradiation time (min)

Figure 5: P h o t o o x i d a t i o n of chlorobenzene calculated by decrease in substrate ( • ) and intermediates d u r i n g p h o t o r c a c t i o n (•)

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Although benzene was not a component of the industrial waste water (see above) it was included in the present work in order to compare it with chlorobenzene. It can be con- cluded from Fig. 6 that in the beginning both photolyses proceed with comparable rates while at later stages the pho- tooxidation of chlorobenzene is less efficient. It is apparently the intermediate which is responsible for this delay (Fig. 6).

0 10 20 30 40 50 irradiation time (min)

F i g u r e 6: P h o t o o x i d a t i o n of benzene calculated by decrease in sub- strate ( • ) a n d intermediates d u r i n g p h o t o r e a c t i o n ( • )

Although we made no attempt to analyze the intermediates other investigators identified some primary photooxidation products of aromatic compounds. For example, phenol and quinone were formed as intermediates of the photooxidation of benzene [10]. Hydroxylated aromatic compounds were also detected during the photooxidation of substituted ar- omatics [8, 11, 21, 23, 25, 26, 31]. On the basis of our results we can conclude that in the initial attack of O H " radicals there is some discrimination between chlorobenzene and benzene. However, at later stages the disruption of the car- bon-chlorine bonds of chlorobenzene is apparently less facile than the photooxidative breakage of carbon-hydrogen bonds.

While trichloroethylene displays a similar reactivity as chlo- robenzene or benzene (Fig. 7) the photooxidation of tri- chloromethane occurs in one step since no intermediates were detected in the latter case. At any time of the photolysis the decrease of substrate matched the stoichiometric for- mation of C O:. For trichloroethylene the aldehyde CI3CCHO was identified as intermediate of the photooxi- dation [30].

0 10 20 30 40 50 60 irradiation time (min)

F i g u r e 7: P h o t o o x i d a t i o n of trichloroethylene calculated by de- crease of substrate ( • ) a n d intermediates d u r i n g p h o t o r e a c t i o n (•)

T a b l e 2: E x p e r i m e n t a l and theoretical equivalents for the oxygen c o n s u m p t i o n and c a r b o n d i o x i d e p r o d u c t i o n a c c o r d i n g to equation (1) at complete p h o t o o x i d a t i o n

O x y g e n equivalents C O: equivalents Substrate E x p e r i m e n t a l T h e o r e t i - E x p e r i m e n t a l T h e o r e t i -

cal cal

C h l o r o -

benzene 6.0 ± 1 . 0 7.0 5.7 + 0.3 6.0

T r i c h l o r o -

ethylene 1 . 6 ± 0 . 7 1.5 2.1 ± 0 . 2 2.0

T r i c h l o r o -

methane 0.5 + 0.3 0.5 1.1 ± 0 . 2 1.0

Benzene 6.4+1.1 7.5 6.0 ± 0 . 3 6.0

A complete photooxidation of chlorobenzene, benzene, tri- chloroethylene and trichloromethane was confirmed. At the end of the photolysis the consumption of substrate and ox- ygen matched the formation of C O i according to equation (1) (Table 2).

4 Conclusion

Although more studies are necessary to fully understand the photocatalytic oxidation of organic compounds including chlorinated hydrocarbons a technical application of this method for the decontamination of waste water seems fea- sible.

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Acknowledgement

We thank the Wacker-Chemie G m b H , Burghausen for sup- ply of waste water and Dr. I. Bauer and J. Lenz for help and discussion. Financial support by the Bundesminister für Forschung und Technologie ( B M F T 02-WA 8615) is grate- fully acknowledged. We thank the Degussa A G , Frankfurt for providing titanium dioxide P-25.

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a n d C C 14 w i t h I l l u m i n a t e d T i 02. J o u r n a l of C a t a l y s i s 82, 4 1 8 - 4 2 3 (1983).

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